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Chemical Structure| 1059172-92-7 Chemical Structure| 1059172-92-7

Structure of 1059172-92-7

Chemical Structure| 1059172-92-7

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Product Details of [ 1059172-92-7 ]

CAS No. :1059172-92-7
Formula : C12H16N2O2
M.W : 220.27
SMILES Code : O=C(N1CC2=NC=CC=C2C1)OC(C)(C)C
MDL No. :MFCD19688666

Safety of [ 1059172-92-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

Application In Synthesis of [ 1059172-92-7 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1059172-92-7 ]

[ 1059172-92-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1059172-92-7 ]
  • [ 186203-81-6 ]
YieldReaction ConditionsOperation in experiment
65% With palladium 10% on activated carbon; hydrogen; In 2-methoxy-ethanol; at 70℃; for 6.0h; To a solution of tert-butyl 5H-pyrrolo[3,4-b]pyridine-6(7H)-carboxylate (1.50 g) in glycol monomethyl ether was added a catalytic amount of 10% Pd/C. The suspension was heated to 70 C. and stirred for 6 h under H2. The resulted mixture was cooled to rt, poured into 100 mL of water and extracted with CH2Cl2 (50 mL×3). The combined organic phases were dried over anhydrous Na2SO4 and filtered. The filtrate was concentrated in vacuo to give the title compound as pale yellow oil (0.95 g, 65.00%). The crude product was used for the next step without further purification. The compound was characterized by the following spectroscopic data: MS (ESI, pos. ion) m/z: 227.2 (M+1).
With palladium 10% on activated carbon; hydrogen; In 2-methoxy-ethanol; at 70℃; for 6.0h; To a solution of ier/-butyl 5H-pyrrolo[3,4-b]pyridine-6(7H)- carboxylate (1.50 g) in glycol monomethyl ether was added a catalytic amount of 10 % Pd/C. The suspension was heated to 70 C and stirred for 6 h under H2. The resulted mixture wascooled to rt, poured into 100 mL of water and extracted with CH2C12 (50 mL><3). The combined organic phases were dried over anhydrous Na2S04 and filtered. The filtrate was concentrated in vacuo to give the title compound as pale yellow oil (0.95 g, 65.00 %). The crude product was used for the next step without further purification.The compound was characterized by the following spectroscopic data: MS (ESI, pos. ion) m/z: 227.2 (M+l).
 

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